Crystal Structure of KRAS4b (GMPPNP-bound) in complex with the RBD-PH domains of SIN1. Determined by X-ray diffraction at 2.35 Å resolution. Released 4 Aug 2021.
Explore 7LC1 in 3D Show helices and sheets RCSB PDB PDBe
7LC1 contains 28 α-helices and 41 β-strands across 4 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 2-10 | 9 | 1 |
| α-helix | 16-25 | 10 | |
| β-strand | 37-46 | 10 | 1 |
| β-strand | 49-58 | 10 | 1 |
| α-helix | 62-67 | 6 | |
| α-helix | 68-74 | 7 | |
| β-strand | 77-83 | 7 | 1 |
| α-helix | 87-91 | 5 | |
| α-helix | 93-103 | 11 | |
| β-strand | 111-116 | 6 | 1 |
| α-helix | 127-137 | 11 | |
| β-strand | 141-143 | 3 | 1 |
| β-strand | 145 | 1 | 2 |
| β-strand | 150 | 1 | 2 |
| α-helix | 152-166 | 15 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 279-285 | 7 | 1 |
| β-strand | 288-294 | 7 | 1 |
| β-strand | 300 | 1 | 3 |
| α-helix | 301-313 | 13 | |
| β-strand | 323-327 | 5 | 1 |
| β-strand | 340 | 1 | 3 |
| β-strand | 348-353 | 6 | 1 |
| α-helix | 358-360 | 3 | |
| α-helix | 369-370 | 2 | |
| α-helix | 371-378 | 8 | |
| β-strand | 384-392 | 9 | 4 |
| β-strand | 396-404 | 9 | 4 |
| β-strand | 408-413 | 6 | 4 |
| α-helix | 425-429 | 5 | |
| β-strand | 430-433 | 4 | 4 |
| α-helix | 434-436 | 3 | |
| β-strand | 437-447 | 11 | 4 |
| β-strand | 450-458 | 9 | 4 |
| β-strand | 463-470 | 8 | 4 |
| α-helix | 472-486 | 15 | |
| α-helix | 493-499 | 7 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3-10 | 8 | 5 |
| α-helix | 16-25 | 10 | |
| β-strand | 37-46 | 10 | 5 |
| β-strand | 49-58 | 10 | 5 |
| α-helix | 59 | 1 | |
| α-helix | 62-67 | 6 | |
| α-helix | 68-74 | 7 | |
| β-strand | 77-83 | 7 | 5 |
| α-helix | 87-103 | 17 | |
| β-strand | 111-116 | 6 | 5 |
| α-helix | 127-137 | 11 | |
| β-strand | 141-143 | 3 | 5 |
| α-helix | 152-164 | 13 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 279-285 | 7 | 5 |
| β-strand | 288-294 | 7 | 5 |
| β-strand | 300 | 1 | 6 |
| α-helix | 301-313 | 13 | |
| β-strand | 323-327 | 5 | 5 |
| α-helix | 333 | 1 | |
| β-strand | 334 | 1 | 5 |
| α-helix | 335 | 1 | |
| β-strand | 340 | 1 | 6 |
| β-strand | 348-353 | 6 | 5 |
| α-helix | 369-370 | 2 | |
| α-helix | 371-378 | 8 | |
| β-strand | 384-392 | 9 | 7 |
| β-strand | 396-404 | 9 | 7 |
| β-strand | 408-413 | 6 | 7 |
| β-strand | 430-433 | 4 | 7 |
| β-strand | 437-447 | 11 | 7 |
| β-strand | 450-458 | 9 | 7 |
| β-strand | 463-470 | 8 | 7 |
| α-helix | 472-487 | 16 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Isoform 2B of GTPase KRas | A, C | protein | 170 | Homo sapiens | P01116 (AlphaFold model) |
| Target of rapamycin complex 2 subunit MAPKAP1 | B, D | protein | 237 | Homo sapiens | Q9BPZ7 (AlphaFold model) |
>7LC1_1 Isoform 2B of GTPase KRas (chains A, C) GMTEYKLVVVGAGGVGKSALTIQLIANHFVDEYDPTIEDSYRKQVVIDGETCLLDILDTA GQEEYSAMRDQYMRTGEGFLCVFAINNTKSFEDIHHYREQIKRVKDSEDVPMVLVGNKCD LPSRTVDTKQAQDLARSYGIPFIETSAKTRQGVDDAFYTLVREIRKHKEK
>7LC1_2 Target of rapamycin complex 2 subunit MAPKAP1 (chains B, D) GSKESLFVRINAAHGFSLIQVDNTKVTMKEILLKAVKRRKGSQKVSGPQYRLEKQSEPNV AVDLDSTLESQSAWEFCLVRENSSRADGVFEEDSQIDIATVQDMLSSHHYKSFKVSMIHR LRFTTDVQLGISGDKVEIDPVTNQKASTKFWIKQKPISIDSDLLCACDLAEEKSPSHAIF KLTYLSNHDYKHLYFESDAATVNEIVLKVNYILESRASTARADYFAQKQRKLNRRTS
| ID | Name | Formula | Copies |
|---|---|---|---|
| GNP | Phosphoaminophosphonic acid-guanylate ester | C10 H17 N6 O13 P3 | 2 |
| MG | Magnesium ion | Mg | 2 |
RAS interaction with Sin1 is dispensable for mTORC2 assembly and activity. Castel, P., Dharmaiah, S., Sale, M.J. et al. Proc Natl Acad Sci U S A (2021) 118. DOI 10.1073/pnas.2103261118 · PubMed
Other PDB entries of the same protein (UniProt P01116 (AlphaFold model), which also has an AlphaFold model), best resolution first:
MolViewer shows 7LC1 directly in your browser with nothing to install. Switch between cartoon, ball-and-stick, spacefill and surface views, color by chain, secondary structure or B-factor, measure distances, angles and dihedrals, and share or embed the view.